Moffitt Cancer Center
CLINICAL RESEARCH COORDINATOR I
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Moffitt Cancer Center
Summary Are you looking for an opportunity to impact lives and be a central part of a dynamic and innovative team in the fight against cancer? As a Moffitt Clinical Research Coordinator, you’ll bring hope to patients by delivering tomorrow’s cancer treatments today! You will have the opportunity to interact directly with patients, enroll, educate and guide them through the experiences of taking part in clinical trials while receiving innovative treatments as part of a therapeutic clinical trial. You will be the member of the Team that ensures the trial is moving forward safely, smoothly, and according to plan. Our Clinical Research Coordinators come from a variety of backgrounds and experiences, including social sciences, biological sciences, business, and humanities. The Clinical Research Coordinator role is a terrific opportunity for those who have already worked in other areas of healthcare as well as those who are looking for a new and exciting way to contribute through their career.
Position Highlights
Coordinate patient care by collaborating with medical staff and document in accordance with standards and regulatory guidelines with direction of a mentor or supervisor.
Act as liaison between the investigators, Moffitt regulatory staff and the sponsor.
Assist to screen, enroll, and follow study subjects, ensuring protocol compliance and close monitoring while the subjects are on study.
Responsible for data and source documentation and adverse experience reporting.
Perform diverse administrative duties requiring analysis, sound judgment, and a high level of knowledge of study protocol.
Work under general supervision and direction from the supervisor and Principal Investigator to implement and coordinate research, including administrative procedures.
Credentials and Qualifications
Bachelor’s degree (preferred field of study: scientific, health related or business administration program) with one (1) year of relevant clinical, health related, scientific, business or research experience.
In lieu of bachelor’s degree, Associate’s degree with 2 years of relevant clinical, health related, scientific, business or research experience.
CCRP/CCRC or equivalent preferred.
Seniority Level: Entry level
Employment Type: Full-time
Job Function: Research, Analyst, and Information Technology – Hospitals and Health Care
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–
Moffitt Cancer Center
Summary Are you looking for an opportunity to impact lives and be a central part of a dynamic and innovative team in the fight against cancer? As a Moffitt Clinical Research Coordinator, you’ll bring hope to patients by delivering tomorrow’s cancer treatments today! You will have the opportunity to interact directly with patients, enroll, educate and guide them through the experiences of taking part in clinical trials while receiving innovative treatments as part of a therapeutic clinical trial. You will be the member of the Team that ensures the trial is moving forward safely, smoothly, and according to plan. Our Clinical Research Coordinators come from a variety of backgrounds and experiences, including social sciences, biological sciences, business, and humanities. The Clinical Research Coordinator role is a terrific opportunity for those who have already worked in other areas of healthcare as well as those who are looking for a new and exciting way to contribute through their career.
Position Highlights
Coordinate patient care by collaborating with medical staff and document in accordance with standards and regulatory guidelines with direction of a mentor or supervisor.
Act as liaison between the investigators, Moffitt regulatory staff and the sponsor.
Assist to screen, enroll, and follow study subjects, ensuring protocol compliance and close monitoring while the subjects are on study.
Responsible for data and source documentation and adverse experience reporting.
Perform diverse administrative duties requiring analysis, sound judgment, and a high level of knowledge of study protocol.
Work under general supervision and direction from the supervisor and Principal Investigator to implement and coordinate research, including administrative procedures.
Credentials and Qualifications
Bachelor’s degree (preferred field of study: scientific, health related or business administration program) with one (1) year of relevant clinical, health related, scientific, business or research experience.
In lieu of bachelor’s degree, Associate’s degree with 2 years of relevant clinical, health related, scientific, business or research experience.
CCRP/CCRC or equivalent preferred.
Seniority Level: Entry level
Employment Type: Full-time
Job Function: Research, Analyst, and Information Technology – Hospitals and Health Care
#J-18808-Ljbffr